학술논문

Pediatric glioblastoma with oligodendroglioma component: Aggressive clinical phenotype with distinct molecular characteristics.
Document Type
Article
Source
Neuropathology. Dec2013, Vol. 33 Issue 6, p652-657. 6p.
Subject
*GLIOBLASTOMA multiforme
*GLIOMA treatment
*TEMOZOLOMIDE
*GENETIC mutation
*GENETICS
Language
ISSN
0919-6544
Abstract
The 2007 World Health Organization classification defined a new variant of glioblastoma ( GBM) containing oligodendroglioma foci as GBM with an oligodendroglioma component ( GBMO), which shows a favorable clinical outcome compared with 'classic' GBM. However, all of the reported cases of GBMO have been adult cases, with no previous reports of pediatric cases. In this report, we demonstrated molecular characteristics of a pediatric GBMO case, showing aggressive clinical behavior with 8-month overall survival. The case showed neither isocitrate dehydrogenase 1/2 genes ( IDH1/2) mutation nor 1p/19q co-deletion, a hallmark of oligodendroglioal tumors. In addition, microsatellite instability, leading to the putative mechanism of temozolomide ( TMZ) resistance, was frequently detected. Molecular genetic analysis may provide critical prognostic and therapeutic insights, especially for the pediatric glioma containing oligodendroglioma components. [ABSTRACT FROM AUTHOR]